The utility of extended differential parameters as a biomarker of bacteremia at a tertiary academic hospital in persons with and without HIV infection in South Africa
Extended differential parameters (EDPs) are generated with the automated differential count by Sysmex XN-series automated hematology analysers, and include the immature granulocyte count (IG%), the neutrophil fluorescent light intensity (NE-SFL) and the neutrophil fluorescent light distribution widt...
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description | Extended differential parameters (EDPs) are generated with the automated differential count by Sysmex XN-series automated hematology analysers, and include the immature granulocyte count (IG%), the neutrophil fluorescent light intensity (NE-SFL) and the neutrophil fluorescent light distribution width (NE-WY). These have been proposed as early biomarkers of bacteremia. This study aimed to evaluate the NE-SFL, NE-WY and IG% in comparison to neutrophil CD64 (nCD64) expression (as a high quality sepsis biomarker) among patients with suspected bacterial sepsis at the Chris Hani Baragwanath Academic Hospital in Johannesburg, South Africa.
A daily search of the laboratory information system identified samples submitted for a blood culture (BC) and a concurrent full blood count (FBC). Automated differential counts using a Sysmex XN-9000 haematology analyser and neutrophil CD64 expression by flow cytometry were assessed on the residual FBC samples.
A total of 151 samples were collected, of which 83 were excluded due to equivocal results with regards to the presence of bacterial infection. The remaining 68 samples included 23 with bacteremia, 28 with evidence of non-bacteremic bacterial infection, 13 with no evidence of bacterial infection and 4 with Tuberculosis. HIV status was documented in 90 of the patients, with a seropositivity rate of 57.8%. The EDPs were all significantly higher among patients with bacteremia as compared to those without bacterial infection, but on ROC curve analyses, only the NE-SFL showed good performance (AUC>0.8) for discriminating cases with bacteremia from those without bacterial infection at a cut-off value of 49.75. In comparison to the nCD64, the NE-SFL showed moderate agreement (kappa = 0.5). On stratification of the ROC analysis by HIV status, the NE-SFL showed superior performance among persons with HIV infection (AUC = 1), while the automated IG% showed better performance among the patients without HIV infection (AUC = 0.9).
In this study, EDPs showed differential performance as biomarkers for bacteremia according to HIV-status in the South African setting, with the most promising results seen with the NE-SFL and IG% parameters among people with and without HIV infection, respectively. Further assessment of these parameters without pre-selection of patients likely to have infection is required to further determine their clinical utility, particularly among patients with underlying inflammatory conditions or malignancy. |
doi_str_mv | 10.1371/journal.pone.0262938 |
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A daily search of the laboratory information system identified samples submitted for a blood culture (BC) and a concurrent full blood count (FBC). Automated differential counts using a Sysmex XN-9000 haematology analyser and neutrophil CD64 expression by flow cytometry were assessed on the residual FBC samples.
A total of 151 samples were collected, of which 83 were excluded due to equivocal results with regards to the presence of bacterial infection. The remaining 68 samples included 23 with bacteremia, 28 with evidence of non-bacteremic bacterial infection, 13 with no evidence of bacterial infection and 4 with Tuberculosis. HIV status was documented in 90 of the patients, with a seropositivity rate of 57.8%. The EDPs were all significantly higher among patients with bacteremia as compared to those without bacterial infection, but on ROC curve analyses, only the NE-SFL showed good performance (AUC>0.8) for discriminating cases with bacteremia from those without bacterial infection at a cut-off value of 49.75. In comparison to the nCD64, the NE-SFL showed moderate agreement (kappa = 0.5). On stratification of the ROC analysis by HIV status, the NE-SFL showed superior performance among persons with HIV infection (AUC = 1), while the automated IG% showed better performance among the patients without HIV infection (AUC = 0.9).
In this study, EDPs showed differential performance as biomarkers for bacteremia according to HIV-status in the South African setting, with the most promising results seen with the NE-SFL and IG% parameters among people with and without HIV infection, respectively. Further assessment of these parameters without pre-selection of patients likely to have infection is required to further determine their clinical utility, particularly among patients with underlying inflammatory conditions or malignancy.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0262938</identifier><identifier>PMID: 35176042</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Academic Medical Centers - statistics & numerical data ; Adolescent ; Adult ; Analysis ; Automation ; Bacteremia ; Bacteremia - blood ; Bacteremia - diagnosis ; Bacteremia - etiology ; Bacteria ; Bacteria - isolation & purification ; Bacterial diseases ; Bacterial infections ; Biological markers ; Biology and Life Sciences ; Biomarkers ; Biomarkers - blood ; Blood ; Blood Culture ; Child ; Child, Preschool ; Diagnosis ; Female ; Flow cytometry ; Fluorescence ; Granulocytes ; Hematology ; HIV ; HIV - isolation & purification ; HIV infection ; HIV Infections - complications ; HIV Infections - virology ; Hospitals ; Human immunodeficiency virus ; Humans ; Immunoglobulins ; Infant ; Infections ; Inflammation ; Information systems ; Laboratories ; Laboratory information management systems ; Leukocytes (granulocytic) ; Leukocytes (neutrophilic) ; Light distribution ; Light intensity ; Luminous intensity ; Lymphocytes ; Male ; Malignancy ; Medical examination ; Medicine and Health Sciences ; Middle Aged ; Morphology ; Neutrophils ; Parameters ; Patients ; Public health ; ROC Curve ; Sepsis ; Sepsis - blood ; Sepsis - diagnosis ; Sepsis - etiology ; Tertiary ; Tertiary Care Centers - statistics & numerical data ; Tuberculosis ; Young Adult</subject><ispartof>PloS one, 2022-02, Vol.17 (2), p.e0262938</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Lemkus et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Lemkus et al 2022 Lemkus et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-84f130b70609d5d4119a5d491d843622394493886d94ff4170675b59af6cdc373</citedby><cites>FETCH-LOGICAL-c692t-84f130b70609d5d4119a5d491d843622394493886d94ff4170675b59af6cdc373</cites><orcidid>0000-0002-4551-0800</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853519/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853519/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35176042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Manuzak, Jennifer</contributor><creatorcontrib>Lemkus, Lauren</creatorcontrib><creatorcontrib>Lawrie, Denise</creatorcontrib><creatorcontrib>Vaughan, Jenifer</creatorcontrib><title>The utility of extended differential parameters as a biomarker of bacteremia at a tertiary academic hospital in persons with and without HIV infection in South Africa</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Extended differential parameters (EDPs) are generated with the automated differential count by Sysmex XN-series automated hematology analysers, and include the immature granulocyte count (IG%), the neutrophil fluorescent light intensity (NE-SFL) and the neutrophil fluorescent light distribution width (NE-WY). These have been proposed as early biomarkers of bacteremia. This study aimed to evaluate the NE-SFL, NE-WY and IG% in comparison to neutrophil CD64 (nCD64) expression (as a high quality sepsis biomarker) among patients with suspected bacterial sepsis at the Chris Hani Baragwanath Academic Hospital in Johannesburg, South Africa.
A daily search of the laboratory information system identified samples submitted for a blood culture (BC) and a concurrent full blood count (FBC). Automated differential counts using a Sysmex XN-9000 haematology analyser and neutrophil CD64 expression by flow cytometry were assessed on the residual FBC samples.
A total of 151 samples were collected, of which 83 were excluded due to equivocal results with regards to the presence of bacterial infection. The remaining 68 samples included 23 with bacteremia, 28 with evidence of non-bacteremic bacterial infection, 13 with no evidence of bacterial infection and 4 with Tuberculosis. HIV status was documented in 90 of the patients, with a seropositivity rate of 57.8%. The EDPs were all significantly higher among patients with bacteremia as compared to those without bacterial infection, but on ROC curve analyses, only the NE-SFL showed good performance (AUC>0.8) for discriminating cases with bacteremia from those without bacterial infection at a cut-off value of 49.75. In comparison to the nCD64, the NE-SFL showed moderate agreement (kappa = 0.5). On stratification of the ROC analysis by HIV status, the NE-SFL showed superior performance among persons with HIV infection (AUC = 1), while the automated IG% showed better performance among the patients without HIV infection (AUC = 0.9).
In this study, EDPs showed differential performance as biomarkers for bacteremia according to HIV-status in the South African setting, with the most promising results seen with the NE-SFL and IG% parameters among people with and without HIV infection, respectively. Further assessment of these parameters without pre-selection of patients likely to have infection is required to further determine their clinical utility, particularly among patients with underlying inflammatory conditions or malignancy.</description><subject>Academic Medical Centers - statistics & numerical data</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Analysis</subject><subject>Automation</subject><subject>Bacteremia</subject><subject>Bacteremia - blood</subject><subject>Bacteremia - diagnosis</subject><subject>Bacteremia - etiology</subject><subject>Bacteria</subject><subject>Bacteria - isolation & purification</subject><subject>Bacterial diseases</subject><subject>Bacterial infections</subject><subject>Biological markers</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Blood</subject><subject>Blood Culture</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Flow cytometry</subject><subject>Fluorescence</subject><subject>Granulocytes</subject><subject>Hematology</subject><subject>HIV</subject><subject>HIV - isolation & purification</subject><subject>HIV infection</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - virology</subject><subject>Hospitals</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Infant</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Information systems</subject><subject>Laboratories</subject><subject>Laboratory information management systems</subject><subject>Leukocytes (granulocytic)</subject><subject>Leukocytes (neutrophilic)</subject><subject>Light distribution</subject><subject>Light intensity</subject><subject>Luminous intensity</subject><subject>Lymphocytes</subject><subject>Male</subject><subject>Malignancy</subject><subject>Medical examination</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>Morphology</subject><subject>Neutrophils</subject><subject>Parameters</subject><subject>Patients</subject><subject>Public health</subject><subject>ROC Curve</subject><subject>Sepsis</subject><subject>Sepsis - 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statistics & numerical data</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Analysis</topic><topic>Automation</topic><topic>Bacteremia</topic><topic>Bacteremia - blood</topic><topic>Bacteremia - diagnosis</topic><topic>Bacteremia - etiology</topic><topic>Bacteria</topic><topic>Bacteria - isolation & purification</topic><topic>Bacterial diseases</topic><topic>Bacterial infections</topic><topic>Biological markers</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Blood</topic><topic>Blood Culture</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Flow cytometry</topic><topic>Fluorescence</topic><topic>Granulocytes</topic><topic>Hematology</topic><topic>HIV</topic><topic>HIV - isolation & purification</topic><topic>HIV infection</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - virology</topic><topic>Hospitals</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Infant</topic><topic>Infections</topic><topic>Inflammation</topic><topic>Information systems</topic><topic>Laboratories</topic><topic>Laboratory information management systems</topic><topic>Leukocytes (granulocytic)</topic><topic>Leukocytes (neutrophilic)</topic><topic>Light distribution</topic><topic>Light intensity</topic><topic>Luminous intensity</topic><topic>Lymphocytes</topic><topic>Male</topic><topic>Malignancy</topic><topic>Medical examination</topic><topic>Medicine and Health Sciences</topic><topic>Middle Aged</topic><topic>Morphology</topic><topic>Neutrophils</topic><topic>Parameters</topic><topic>Patients</topic><topic>Public health</topic><topic>ROC Curve</topic><topic>Sepsis</topic><topic>Sepsis - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lemkus, Lauren</au><au>Lawrie, Denise</au><au>Vaughan, Jenifer</au><au>Manuzak, Jennifer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The utility of extended differential parameters as a biomarker of bacteremia at a tertiary academic hospital in persons with and without HIV infection in South Africa</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2022-02-17</date><risdate>2022</risdate><volume>17</volume><issue>2</issue><spage>e0262938</spage><pages>e0262938-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Extended differential parameters (EDPs) are generated with the automated differential count by Sysmex XN-series automated hematology analysers, and include the immature granulocyte count (IG%), the neutrophil fluorescent light intensity (NE-SFL) and the neutrophil fluorescent light distribution width (NE-WY). These have been proposed as early biomarkers of bacteremia. This study aimed to evaluate the NE-SFL, NE-WY and IG% in comparison to neutrophil CD64 (nCD64) expression (as a high quality sepsis biomarker) among patients with suspected bacterial sepsis at the Chris Hani Baragwanath Academic Hospital in Johannesburg, South Africa.
A daily search of the laboratory information system identified samples submitted for a blood culture (BC) and a concurrent full blood count (FBC). Automated differential counts using a Sysmex XN-9000 haematology analyser and neutrophil CD64 expression by flow cytometry were assessed on the residual FBC samples.
A total of 151 samples were collected, of which 83 were excluded due to equivocal results with regards to the presence of bacterial infection. The remaining 68 samples included 23 with bacteremia, 28 with evidence of non-bacteremic bacterial infection, 13 with no evidence of bacterial infection and 4 with Tuberculosis. HIV status was documented in 90 of the patients, with a seropositivity rate of 57.8%. The EDPs were all significantly higher among patients with bacteremia as compared to those without bacterial infection, but on ROC curve analyses, only the NE-SFL showed good performance (AUC>0.8) for discriminating cases with bacteremia from those without bacterial infection at a cut-off value of 49.75. In comparison to the nCD64, the NE-SFL showed moderate agreement (kappa = 0.5). On stratification of the ROC analysis by HIV status, the NE-SFL showed superior performance among persons with HIV infection (AUC = 1), while the automated IG% showed better performance among the patients without HIV infection (AUC = 0.9).
In this study, EDPs showed differential performance as biomarkers for bacteremia according to HIV-status in the South African setting, with the most promising results seen with the NE-SFL and IG% parameters among people with and without HIV infection, respectively. Further assessment of these parameters without pre-selection of patients likely to have infection is required to further determine their clinical utility, particularly among patients with underlying inflammatory conditions or malignancy.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>35176042</pmid><doi>10.1371/journal.pone.0262938</doi><tpages>e0262938</tpages><orcidid>https://orcid.org/0000-0002-4551-0800</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2022-02, Vol.17 (2), p.e0262938 |
issn | 1932-6203 1932-6203 |
language | eng |
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source | Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Academic Medical Centers - statistics & numerical data Adolescent Adult Analysis Automation Bacteremia Bacteremia - blood Bacteremia - diagnosis Bacteremia - etiology Bacteria Bacteria - isolation & purification Bacterial diseases Bacterial infections Biological markers Biology and Life Sciences Biomarkers Biomarkers - blood Blood Blood Culture Child Child, Preschool Diagnosis Female Flow cytometry Fluorescence Granulocytes Hematology HIV HIV - isolation & purification HIV infection HIV Infections - complications HIV Infections - virology Hospitals Human immunodeficiency virus Humans Immunoglobulins Infant Infections Inflammation Information systems Laboratories Laboratory information management systems Leukocytes (granulocytic) Leukocytes (neutrophilic) Light distribution Light intensity Luminous intensity Lymphocytes Male Malignancy Medical examination Medicine and Health Sciences Middle Aged Morphology Neutrophils Parameters Patients Public health ROC Curve Sepsis Sepsis - blood Sepsis - diagnosis Sepsis - etiology Tertiary Tertiary Care Centers - statistics & numerical data Tuberculosis Young Adult |
title | The utility of extended differential parameters as a biomarker of bacteremia at a tertiary academic hospital in persons with and without HIV infection in South Africa |
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